Canonical Allele Identifier: PA105637
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 31946
ClinVar RCV Id: RCV000024624 RCV000546897 RCV001270102 RCV001570693 RCV004545734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Arg1154Trp
CA260058
NM_005691.3:c.3460C>T